Package 0832-5323-10

{"route": ["ORAL"], "spl_id": "39e726b1-eab8-fcf4-e063-6394a90a950a", "openfda": {"unii": ["660YQ98I10"], "rxcui": ["312529", "628953"], "spl_set_id": ["616f0de7-8843-44a1-8fa6-274d889286aa"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-10)", "package_ndc": "0832-5323-10", "marketing_start_date": "20190621"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0832-5323-11)", "package_ndc": "0832-5323-11", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "0832-5323_39e726b1-eab8-fcf4-e063-6394a90a950a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0832-5323", "generic_name": "Potassium Chloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "NDA019123", "marketing_category": "NDA", "marketing_start_date": "19860417", "listing_expiration_date": "20261231"}